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The investigation of a series of n-hydroxybenzoic acids (n=p, m, o) on a new surface enhanced Raman scattering active substrate.

Ag nanoparticles, organized on indium tin oxide (ITO) surface, can act as a new surface enhanced Raman scattering (SERS) active substrate as well as a dry electrode. Compared with the traditional SERS-active substrate, its notable advantage is that the microcosmic changes of the film can be reflected by the SERS spectrum during the investigation of the film's electrical and other macroscopic characteristics. To illuminate the above-mentioned property of this new substrate, a series of n-hydroxybenzoic acids (n-HBA; n=p, m and o) was tested as probe molecules by SERS technique. These SERS spectra indicate that the significant changes of frequencies as well as intensities, respectively, arise from the changes of the adsorption behavior along with the proportional variation of molecules and silver nanoparticles. Excellent SERS signals prove that the silver nanoparticles-coated ITO is a highly SERS-active substrate and can efficiently reflect the microcosmic property of the film, which suggest it has promising potential of being a new technique for further application in the field of thin-film research.

Colloids↗

Spectral studies of SnO2 nanofibres prepared by electrospinning method.

Tin oxide nanofibres with 100-150 nm diameter has been prepared, for the first time by calcination of poly(vinyl acetate) (PVAc)/SnO2 composite fibres prepared by electrospinning method as precursor. Scanning electron microscopic images revealed cylindrical morphology of the fibres after calcination at 600 degrees C. Both, X-ray diffraction (XRD) and Raman spectral data confirmed the presence of phase pure tetragonal rutile tin oxide after calcination process. Room temperature photoluminescence (PL) spectra of tin oxide nanofibres under excitation at 325 nm wavelength show a strong green emission at 525 nm with a band gap of 2.41 eV. FT-IR spectra confirmed the formation of pure tin oxide after calcination at 600 degrees C and complete removal of PVAc during calcination. UV-vis spectrum of the fibres showed absorption at 315 nm due to the direct electron transfer in tin oxide.

Crystallization↗

Theoretical study of electronic structures and spectroscopic properties of Ga3Sn, GaSn3, and their ions.

Ground and excited states of mixed gallium stannide tetramers (Ga3Sn, Ga3Sn+, Ga3Sn-, GaSn3, GaSn3+, and GaSn3-) are investigated employing the complete active space self-consistent-field (CASSCF), density function theory (DFT), and the coupled-cluster single and double substitution (including triple excitations) (CCSD(T)) methods. The ground states of Ga3Sn, Ga3Sn+, and Ga3Sn- are found to be the 2A1, 3B1, and 1A1 states in C2v symmetry with a planar quadrilateral geometry, respectively. The ground states of GaSn3 and GaSn3- is predicted to be the 2A1 and 1A1 states in C2v point group with a planar quadrilateral structure, respectively, while the ground state of GaSn3+ is the 1A1 state with ideal triangular pyramid C3v geometry. Equilibrium geometries, vibrational frequencies, binding energies, electron affinities, ionization energies, and other properties of Ga3Sn and GaSn3 are computed and discussed. The anion photoelectron spectra of Ga3Sn- and GaSn3- are also predicted. It is interesting to find that the amount of charge transfer between Ga and Sn2 atoms in the 1A1 state of GaSn3+ greatly increases upon electron ionization from the 2A1 state of GaSn3, which may be caused by large geometry change. On the other hand, the results of the low-lying states of Ga3Sn and GaSn3 are compared with those of Ga3Si and GaSi3.

Gallium↗

Protective role of ascorbic acid to enhance reproductive performance of male rabbits treated with stannous chloride.

The objective of this study was to determine the protective role of ascorbic acid (AA, 40 mg/kg BW) on reproductive performance of male New Zealand White rabbits given sublethal dose (20 mg/kg BW every other day for 12 weeks) of stannous chloride (SnCl2). Results showed that treatment with SnCl2 caused a decrease (P<0.05) in libido (by increasing the reaction time), ejaculate volume, sperm concentration, total sperm output, sperm motility (%), total motile sperm per ejaculate (TMS), packed sperm volume (PSV), total functional sperm fraction (TFSF), normal and live sperm and semen initial fructose. Dead sperm and initial hydrogen ion concentration (pH) were increased. While, relative weights of testes (RTW) and epididymis (REW) were decreased. On the other hand, live body weight (LBW) and dry matter intake (DMI) did not change. Treatment with AA alone caused significant increase in LBW, DMI, RTW, REW and semen characteristics compared to control group. Also, the presence of AA with SnCl2 minimized its harmful effects. Results obtained revealed suggest that assessment of reproductive toxicity of stannous chloride needs to be addressed, and may presently be underestimated. Also, the beneficial influences of AA in counteracting the toxic effects of SnCl2 and improved the reproductive performance of male rabbit was demonstrated.

Animals↗

Effect of metal chlorides on thermal degradation of (waste) polycarbonate.

In this study, we investigated how to treat (waste) polycarbonate efficiently to reduce its degraded residue. The study was carried out in an isothermal reactor under continuous nitrogen flow at atmospheric pressure to pyrolyze polycarbonate (PC) alone and in the presence of metal chloride. Some metal chlorides were shown to be catalytic active for the degradation of PC at 400 degrees C, which increased degradation conversion from 8.5% to more than 58.3%. Among those active metal chlorides, ZnCl2 and SnCl2 can produce higher liquid product yields. Effects such as particle size of PC, temperature, the weight ratio of metal chloride/PC, and degradation time on the degradation conversion of PC without and with these two most active metal chlorides were studied. Results of the liquid product analysis by GC/MS demonstrated the product composition of PC degradation over the metal chlorides is much simpler than that of degradation alone. The main liquid product is phenol, p-isopropylphenol, diphenyl carbonate, and bisphenol A for all cases.

Catalysis↗

Rapid pH change due to bacteriorhodopsin measured with a tin-oxide electrode.

The photocurrent transient generated by bacteriorhodopsin (bR) on a tin-oxide electrode is due to pH change and not to charge displacement as previously assumed. Films of either randomly oriented or highly oriented purple membranes were deposited on transparent electrodes made of tin-oxide-coated glass. The membranes contained either wild-type or D96N-mutant bR. When excited with yellow light through the glass, the bR pumps protons across the membrane. The result is a rapid local pH change as well as a charge displacement. Experiments with these films show that it is the pH change rather than the displacement that produces the current transient. The calibration for the transient pH measurement is given. The sensitivity of a tin-oxide electrode to a transient pH change is very much larger than its sensitivity to a steady-state pH change.

Bacteriorhodopsins↗

Order in phospholipid Langmuir-Blodgett layers and the effect of the electrical potential of the substrate.

The ordering in dipalmitoylphosphatidylcholine (DPPC) Langmuir-Blodgett monolayers and bilayers on a semiconducting indium tin oxide (ITO) surface has been investigated at the equilibrium potential of the interface and at various externally applied potentials. Second- and fourth-rank order parameters of a diphenylhexatriene (DPH) containing phospholipid probe were derived from total internal reflection fluorescence measurements, and orientation distributions were calculated using the maximum-entropy method. Generally, bimodal orientation distributions were obtained, suggesting that only part of the probes is aligned with the DPPC molecules. The effect of applied potentials is small for DPPC layers on unmodified (hydrophilic) ITO; with decreasing potential the ordering changes slightly to more random distributions, possibly because of the onset of hydrogen evolution at the substrate surface. For monolayers on hydrophobized ITO, where the phospholipids are initially with their tails directed toward the surface, the changes are more significant. At the highest positive potential applied, the derived order parameters indicate that nearly all probes are flat on the surface. This can be understood as a result of enhanced competition between headgroups and tails for access to the surface as it becomes more polarized. On unmodified ITO the electrochemistry of Fe(CN)6(3-/4-) and Ru(bipyridyl)3(2+/3+) is hardly hindered by the presence of DPPC monolayers or bilayers. On hydrophobized ITO a DPPC monolayer enhances the redox reactions.

1,2-Dipalmitoylphosphatidylcholine↗

Differential acute effects of fluoxetine on frontal and auditory cortex networks in vitro.

Primary cultures of neuronal networks grown on microelectrode arrays were used to quantify acute effects of fluoxetine (Prozac) on spontaneous spike and burst activity. For frontal cortex cultures, fluoxetine showed consistent inhibitory effects and terminated activity at 10-16 microM. IC(50) mean+/-S.E. for spike rates was 5.4+/-0.7 microM (n=15). For auditory cortex cultures, fluoxetine caused excitation at 1-10 microM, initial inhibition at 15 microM, and activity cessation at 20-25 microM. The spike rate IC(50) was 15.9+/-1.0 microM (n=11). Fluoxetine did not change the action potential waveform shape. However, at high concentrations, it caused total cessation of spike activity on all channels. The inhibition caused by fluoxetine was reversible for both tissues. Based on the results, we conclude that cultures showed repeatable, concentration-dependent sensitivities to fluoxetine but demonstrated tissue-specific responses for frontal and auditory cortex networks. These responses may not be due to the interference with serotonin reuptake, but may be due to a secondary effect on ionic channels.

Action Potentials↗

Case report: investigation of chyluria.

We present a case of chyluria in which the demonstration of abnormal lymphaticourinary communication was established by conventional lymphangiography. Radiocolloid lymphoscintigraphy failed to demonstrate the site of leakage, probably due to technical factors which are discussed.

Chyle↗

SnO2 thin films prepared by dip-coating from microwave synthesized colloidal suspensions.

Tin(IV) oxide thin films have been prepared by dip-coating. The suspensions used for these depositions have been synthesized by microwave-induced thermohydrolysis of tin tetrachloride aqueous solutions in the presence of hydrochloric acid. Single or multiple depositions were tested, on glass substrates as well as on pure SiO2. The obtained thin films were characterized by optical microscopy, interferometric roughness measurements (Micromap), scanning electron microscopy, secondary ion mass spectroscopy, and scanning tunneling microscopy.

Colloids↗

The qualitative effects of various types of hygiene instrumentation on commercially pure titanium and titanium alloy implant abutments: an in vitro and scanning electron microscope study.

STATEMENT OF PROBLEM: Implant survival depends on proper and timely oral hygiene maintenance, and a wide variety of oral prophylaxis procedures have been recommended and used on implant abutments. PURPOSE: This in vitro study compared the surface quality of both commercially pure titanium and titanium-alloy implant abutments, subjected to various hygiene methods and instruments with a standardized, clinically applicable scaling force. MATERIAL AND METHODS: Commercially pure titanium and titanium-alloy abutments were exposed to five oral hygiene methods; a gold-alloy-tipped scaler, a high-grade resin scaler, a graphite-reinforced scaler, an air-powder abrasive system, and a rubber cup with tin oxide slurry. A customized test device that simulated the scaling motion and allowed the application of a standard load at the tip of the scaler was used. Scanning electron photomicrographs (x200) of the pretreatment and treated surfaces were obtained and compared qualitatively. RESULTS AND CONCLUSIONS: No significant surface alteration was produced by the air abrasive system. All other hygiene methods either created significant surface alterations, left residual particles on the abutment surfaces, or both.

Acrylic Resins↗

Bond strengths of resin-to-metal bonding systems.

STATEMENT OF PROBLEM: Resinous materials for the veneers of fixed prostheses commonly require mechanical retention on metal substructures because there is no chemical adhesion. However, mechanical retention does not restrict creation of a marginal gap at the resin-metal interface, which can cause discoloration or detachment of resinous material. The development of a chemical resin-to-metal bonding could resolve this problem and also reduce the need for mechanical retention (pearls, wires) on metal frameworks. PURPOSE: This study evaluated six current methods with the use of various storage conditions to predict clinical efficacy. MATERIAL AND METHODS: Six resin-to-metal bonding systems were tested: Silicoater, Silicoater MD, Rocatec, OVS, Sebond, and Spectra-Link. All specimens were examined in bending tests after 24 hours of dry storage (category A), after 24 hours of water storage and thermocycling (category B), and after 2 months of water storage and thermocycling (category C). Tensional tests were completed for all bonding systems after dry storage, and microscopic examination (optical and SEM) was performed for all specimens. RESULTS AND CONCLUSIONS: This study indicated that certain systems can provide stable bonding of resin to metal substructures despite prolonged wet storage and intensive thermocycling. These systems can also be used clinically without retentive configurations on metal frameworks, resulting in better esthetics. Some bonding systems revealed progressive weakening of bond strengths, so research is needed to verify their clinical efficacy.

Dental Alloys↗

Induction of heme oxygenase produces load-independent cardioprotective effects in hypertensive rats.

Although heme oxygenase (HO) has been suggested to be involved in the regulation of cardiovascular function through production of carbon monoxide (CO), the pathophysiological significance of HO in hypertensive organ damage remains unknown. We examined the effects of inducing HO-1 mRNA by stannous chloride (SnCl2) on cardiac hypertrophy in stroke-prone spontaneously hypertensive rats (SHR-SP/Izm). Chronic administration of SnCl2 resulted in a significant decrease in left ventricular (LV) weight/body weight ratio and LV brain natriuretic peptide (BNP) mRNA levels as a marker of cardiac hypertrophy and a significant increase in LV HO-1 mRNA levels and LV cGMP contents in SHR-SP/Izm, while there was no significant change in systemic blood pressure. These results provide the first evidence that induction of HO in the heart attenuates cardiac hypertrophy in load-independent mechanism in genetically hypertensive rats.

Animals↗

Immobilization of heavy metals from aqueous solutions using polyacrylamide grafted hydrous tin (IV) oxide gel having carboxylate functional groups.

A new adsorbent containing a carboxylate group has been prepared by the surface modification of a polyacrylamide grafted hydrous tin (IV) oxide gel. The product exhibits a very high adsorption potential for Pb(II), Hg(II) and Cd(II). The effect of initial metal ion concentration, adsorbent dose, pH, concentration of light metal ions, and temperature on metal removal has been studied. The process follows a first-order rate kinetics. The intraparticle diffusion of metal ions through pores in the adsorbent was shown to be the main rate limiting step. The equilibrium data fit well with the Langmuir adsorption isotherm. The selectivity order of the adsorbent is Pb(II) > Hg(II) > Cd(II). Adsorption rate constants and thermodynamic parameters were also presented to predict the nature of adsorption. The method was applied on synthetic wastewaters. Acid regeneration has been tried for several cycles with a view to recover the adsorbed metal ions and also to restore the sorbent to its original state.

Adsorption↗

Composite tin and zinc oxide nanocrystalline particles for enhanced charge separation in sensitized degradation of dyes.

Composite ZnO/SnO2 catalyst has been studied for the sensitized degradation of dyes e.g. Eosin Y (2', 4', 5', 7'-tetrabromofluorescein disodium salt) in relation to efficient charge separation properties of the catalyst. Improved photocatalytic activity was observed in the case of ZnO/SnO2 composite catalyst compared to the catalytic activity of ZnO, SnO2 or TiO2 powder. The suppression of charge recombination in the composite ZnO/SnO2 catalyst led to higher catalytic activity for the degradation of Eosin Y. Degradation of Eosin follows concomitant formation of CO2 and formation of CO2 followed a pseudo-first-order rate. Photoelectrochemical cells constructed using SnO2, ZnO, ZnO/SnO2 sensitized with Eosin Y showed V(oc) of 175, 306, 512 mV/cm2 and I(sc) of 50, 70, 200 microA/cm2 respectively. A higher irreversible degradation of Eosin Y and higher V(oc) observed on composite ZnO/SnO2 than ZnO and SnO2 separately can be considered as a proof of enhanced charge separation of ZnO/SnO2 catalyst. Eosin Y showed a higher emission decreases on ZnO/SnO2 composite than on individual ZnO, SnO2 or TiO2 indicating dominance of the charge injection process. Photoinjected electrons are tunneled from ZnO to SnO2 particles accumulating injected electrons in the conduction bands allowing wider separation of excited carriers.

Catalysis↗

Assessment of tin and butyltin species in estuarine superficial sediments from Gipuzkoa, Spain.

Ten superficial sediments from river estuaries of Gipuzkoa (North Spain) were collected and analyzed for nine metals (including tin, Sn) and butyltin compounds (monobutyltin, MBT; dibutyltin, DBT; tributyltin, TBT). Total metal concentration in the fine fraction (<63 micrometer) of the sediment was determined in aqua regia--hydrofluoric acid extracts by atomic absorption spectrometry. The butyltin species (BTs) were firstly extracted from the sediments with hydrochloric acid-methanol mixture. After derivatization with sodium tetraethyl borate, the organotin compounds were extracted by solid phase microextraction (SPME) in headspace mode. A fiber coated with 100 micrometer poly(dimethylsiloxane) was used for SPME. The organotin species were analyzed by gas chromatography-flame ionization detection. Analysis of the certified reference sediment (PACS-2) shown the suitability of the procedures for determination of metal contents and DBT-TBT species in contaminated sediments. Factorial analysis was used to examine the main sources of metals. Three factors represented more than 89% of the total variance of the metal system, and the Sn was related with Cu-Zn-Pb suggesting the same pollution source. The BTs concentrations in the area were high (TBT ranged from 0.05 to 5.48 mg Sn kg(-1)). The percentage of total butyltin species ( summation operator BTs) respect to the total Sn amount was higher than 4% in all the sediments, showing in the Bidasoa river estuary a remarkable value higher than 20%. Hence, the studied estuarine sediments reflect a pollution that is related with historical industrial and fishing activities of the area.

Environmental Monitoring↗

Magnetron sputtered tin coatings on unbiased ceramic substrates.

OBJECTIVES: The aim of this work was to study the application of tin oxide coatings on alumina, with a view to developing improved bonding for high-alumina dental ceramics. METHODS: By use of a magnetron sputtering technique, alumina was coated with tin which was subsequently oxidized, and the bond strength of coated surfaces to a resin-based dental cement was measured in tension. Tensile bond strength data were assessed for their degree of skewness and the homogeneity of the residual variances with a view to applying appropriate transformations prior to performing ANOVA with subsequent Tukey's analysis as necessary. The color of coatings, as a function of the amount of oxidation of the surface, was noted. Coatings were characterized by SEM and EDAX. It has been found possible to produce esthetic tin oxide coatings on alumina using a simplified magnetron sputtering apparatus in conjunction with post-deposition oxidation. RESULTS: Although mean tensile bond strength (TBS) values in excess of 15 MPa were recorded for a number of groups, no causal relationship was found between coating time and mean TBS. SIGNIFICANCE: The need exists for improved bonding of alumina-based ceramics; further development of a magnetron sputtering technique may provide the means for achieving this.

Aluminum Oxide↗